CP-615,003
From Wikipedia, the free encyclopedia
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Systematic (IUPAC) name | |
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N-(3-fluoro-4-(2-(propylamino)ethoxy)phenyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide
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Identifiers | |
CAS Number | 329016-45-7 ![]() |
PubChem | CID 9820874 |
ChemSpider | 7996623 ![]() |
Chemical data | |
Formula | C20H24FN3O3 |
Molar mass | 373.421 g/mol |
3D model (Jmol) | Interactive image |
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CP-615,003 is a drug which acts as a subtype-selective partial agonist at GABAA receptors, and was developed by Pfizer as a potential anxiolytic; however, poor blood–brain barrier penetration make it primarily useful as a research ligand.[1][2]
References[edit]
- ^ Shaffer CL, Gunduz M, O'Connell TN, Obach RS, Yee S (November 2005). "Biotransformation of a GABAA receptor partial agonist in sprague-dawley rats and cynomolgus monkeys: identification of two unique N-carbamoyl metabolites". Drug Metabolism and Disposition: the Biological Fate of Chemicals. 33 (11): 1688–99. doi:10.1124/dmd.105.004630. PMID 16081672.
- ^ Venkatakrishnan K, Tseng E, Nelson FR, Rollema H, French JL, Kaplan IV, Horner WE, Gibbs MA (August 2007). "Central nervous system pharmacokinetics of the Mdr1 P-glycoprotein substrate CP-615,003: intersite differences and implications for human receptor occupancy projections from cerebrospinal fluid exposures". Drug Metabolism and Disposition: the Biological Fate of Chemicals. 35 (8): 1341–9. doi:10.1124/dmd.106.013953. PMID 17470526.